Chaudhary Mohammed Wajid, Al-Baradie Raidah Saleem
Pediatric Neurology, Neurosciences Centre, King Fahad Specialist Hospital, Dammam, Kingdom of Saudi Arabia.
Appl Clin Genet. 2014 Sep 10;7:159-67. doi: 10.2147/TACG.S35759. eCollection 2014.
Ataxia-telangiectasia (A-T) is an autosomal recessive multi-system disorder caused by mutation in the ataxia-telangiectasia mutated gene (ATM). ATM is a large serine/threonine protein kinase, a member of the phosphoinositide 3-kinase-related protein kinase (PIKK) family whose best-studied function is as master controller of signal transduction for the DNA damage response (DDR) in the event of double strand breaks (DSBs). The DDR rapidly recognizes DNA lesions and initiates the appropriate cellular programs to maintain genome integrity. This includes the coordination of cell-cycle checkpoints, transcription, translation, DNA repair, metabolism, and cell fate decisions, such as apoptosis or senescence. DSBs can be generated by exposure to ionizing radiation (IR) or various chemical compounds, such as topoisomerase inhibitors, or can be part of programmed generation and repair of DSBs via cellular enzymes needed for the generation of the antibody repertoire as well as the maturation of germ cells. AT patients have immunodeficiency, and are sterile with gonadal dysgenesis as a result of defect in meiotic recombination. In the cells of nervous system ATM has additional role in vesicle dynamics as well as in the maintenance of the epigenetic code of histone modifications. Moderate levels of ATM are associated with prolonged lifespan through resistance to oxidative stress. ATM inhibitors are being viewed as potential radiosensitizers as part of cancer radiotherapy. Though there is no cure for the disease at present, glucocorticoids have been shown to induce alternate splicing site in the gene for ATM partly restoring its activity, but their most effective timing in the disease natural history is not yet known. Gene therapy is promising but large size of the gene makes it technically difficult to be delivered across the blood-brain barrier at present. As of now, apart from glucocorticoids, use of histone deacetylase inhibitors/EZH2 to minimize effect of the absence of ATM, looks more promising.
共济失调毛细血管扩张症(A-T)是一种常染色体隐性多系统疾病,由共济失调毛细血管扩张症突变基因(ATM)突变引起。ATM是一种大型丝氨酸/苏氨酸蛋白激酶,属于磷酸肌醇3激酶相关蛋白激酶(PIKK)家族,其研究最深入的功能是在双链断裂(DSB)情况下作为DNA损伤反应(DDR)信号转导的主控制器。DDR能快速识别DNA损伤,并启动适当的细胞程序以维持基因组完整性。这包括细胞周期检查点、转录、翻译、DNA修复、代谢以及细胞命运决定(如凋亡或衰老)的协调。DSB可由暴露于电离辐射(IR)或各种化合物(如拓扑异构酶抑制剂)产生,也可作为通过产生抗体库和生殖细胞成熟所需的细胞酶进行DSB程序性生成和修复的一部分。AT患者存在免疫缺陷,由于减数分裂重组缺陷,性腺发育不全导致不育。在神经系统细胞中,ATM在囊泡动力学以及组蛋白修饰表观遗传密码的维持中具有额外作用。适度水平的ATM通过对氧化应激的抗性与延长寿命相关。ATM抑制剂作为癌症放疗的一部分被视为潜在的放射增敏剂。尽管目前尚无治愈该疾病的方法,但已证明糖皮质激素可诱导ATM基因中的可变剪接位点,部分恢复其活性,但其在疾病自然史中最有效的时机尚不清楚。基因治疗前景广阔,但目前该基因的大尺寸使其在技术上难以跨越血脑屏障进行递送。截至目前,除了糖皮质激素外,使用组蛋白去乙酰化酶抑制剂/EZH2来最小化ATM缺失的影响似乎更有前景。